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Cited by in F6Publishing
For: Liang Y, Du C, Wei H, Zhang C, Zhang M, Hu M, Fang F, Luo X. Genotypic and clinical analysis of 49 Chinese children with hepatic glycogen storage diseases. Mol Genet Genomic Med 2020;8:e1444. [PMID: 32772503 DOI: 10.1002/mgg3.1444] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Du C, Li Z, Wei H, Zhang M, Hu M, Zhang C, Luo X, Liang Y. Clinical analysis and long-term treatment monitoring of 3 patients with glycogen storage disease type Ib. BMC Med Genomics 2021;14:81. [PMID: 33731098 DOI: 10.1186/s12920-021-00936-9] [Reference Citation Analysis]
2 Ahmed S, Akbar F, Ali AJ, Afroze B. Clinical, pathological and molecular spectrum of patients with glycogen storage diseases in Pakistan. J Pediatr Endocrinol Metab 2022. [PMID: 34989216 DOI: 10.1515/jpem-2021-0575] [Reference Citation Analysis]
3 Mori T, Ishikawa A, Shigetomi H, Fukuda T, Sugie H. A novel PHKA2 variant in a Japanese boy with glycogen storage diseases type IXa. Pediatr Int 2021. [PMID: 34837663 DOI: 10.1111/ped.14839] [Reference Citation Analysis]
4 Liang Y, Du C, Wei H, Zhang C, Zhang M, Hu M, Fang F, Luo X. Genotypic and clinical analysis of 49 Chinese children with hepatic glycogen storage diseases. Mol Genet Genomic Med 2020;8:e1444. [PMID: 32772503 DOI: 10.1002/mgg3.1444] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Grünert SC, Hannibal L, Spiekerkoetter U. The Phenotypic and Genetic Spectrum of Glycogen Storage Disease Type VI. Genes (Basel) 2021;12:1205. [PMID: 34440378 DOI: 10.3390/genes12081205] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]